Proper conditional analysis in the presence of missing data: Application to large scale meta-analysis of tobacco use phenotypes

Exome Sequencing Analysis in Severe, Early-Onset Chronic Obstructive Pulmonary Disease

(2016) Dandi Qiao et al.   AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE

RVTESTS: an efficient and comprehensive tool for rare variant association analysis using sequence data: Table 1.

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FINEMAP: efficient variable selection using summary data from genome-wide association studies

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Incorporating Functional Annotations for Fine-Mapping Causal Variants in a Bayesian Framework Using Summary Statistics

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A reference panel of 64,976 haplotypes for genotype imputation

(2016)   NATURE GENETICS

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(2016) Sayantan Das et al.   NATURE GENETICS

Joint Bayesian inference of risk variants and tissue-specific epigenomic enrichments across multiple complex human diseases

(2016) Yue Li et al.   NUCLEIC ACIDS RESEARCH

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(2016) Daisuke Yoneoka et al.   Research Synthesis Methods

Meta-analysis for Discovering Rare-Variant Associations: Statistical Methods and Software Programs

(2015) Zheng-Zheng Tang et al.   AMERICAN JOURNAL OF HUMAN GENETICS

A global reference for human genetic variation

(2015) Richard A. Gibbs et al.   NATURE

LD Score regression distinguishes confounding from polygenicity in genome-wide association studies

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Rare variant genotype imputation with thousands of study-specific whole-genome sequences: implications for cost-effective study designs

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Meta-Analysis of Sequencing Studies With Heterogeneous Genetic Associations

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Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction

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Loss-of-Function Mutations in APOC3, Triglycerides, and Coronary Disease

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Meta-analysis of Gene-Level Associations for Rare Variants Based on Single-Variant Statistics

(2013) Yi-Juan Hu et al.   AMERICAN JOURNAL OF HUMAN GENETICS

General Framework for Meta-analysis of Rare Variants in Sequencing Association Studies

(2013) Seunggeun Lee et al.   AMERICAN JOURNAL OF HUMAN GENETICS

MASS: meta-analysis of score statistics for sequencing studies

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Rare Nonsynonymous Exonic Variants in Addiction and Behavioral Disinhibition

(2013) Scott I. Vrieze et al.   BIOLOGICAL PSYCHIATRY

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(2013) Dajiang J Liu et al.   NATURE GENETICS

Common variants associated with plasma triglycerides and risk for coronary artery disease

(2013) Ron Do et al.   NATURE GENETICS

The NHGRI GWAS Catalog, a curated resource of SNP-trait associations

(2013) Danielle Welter et al.   NUCLEIC ACIDS RESEARCH

Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits

(2012) Jian Yang et al.   NATURE GENETICS

The Minnesota Center for Twin and Family Research Genome-Wide Association Study

(2012) Michael B. Miller et al.   Twin Research and Human Genetics

Sequence variants at CHRNB3–CHRNA6 and CYP2A6 affect smoking behavior

(2010) Thorgeir E Thorgeirsson et al.   NATURE GENETICS

Multiple Independent Loci at Chromosome 15q25.1 Affect Smoking Quantity: a Meta-Analysis and Comparison with Lung Cancer and COPD

(2010) Nancy L. Saccone et al.   PLoS Genetics

Multilocus Bayesian Meta-Analysis of Gene-Disease Associations

(2009) Paul J. Newcombe et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Changes in Insulin Sensitivity and Insulin Release in Relation to Glycemia and Glucose Tolerance in 6,414 Finnish Men

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Bayesian Meta-Analysis of Genetic Association Studies with Different Sets of Markers

(2008) Claudio Verzilli et al.   AMERICAN JOURNAL OF HUMAN GENETICS